Institutional Registry of Hyponatremia
The recruitment status of this study is unknown because the information has not been verified recently.
Verified November 2006 by Hospital Italiano de Buenos Aires.
Recruitment status was Recruiting
Recruitment status was Recruiting
Sponsor:
Hospital Italiano de Buenos Aires
Information provided by:
Hospital Italiano de Buenos Aires
ClinicalTrials.gov Identifier:
NCT01370473
First received: May 2, 2011
Last updated: June 9, 2011
Last verified: November 2006
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Purpose
The purpose of this study is to create a population-based registry system Hyponatremia prospective epidemiological survey of
risk factors, diagnosis, prognosis, treatment, monitoring, survival. This study will also describe the occurrence of hyponatremia in the population of HIBA in the Central Hospital, as well as describe the characteristics of clinical presentation, evolution and predisposing factors of hyponatremia.
| Condition |
|---|
|
Hyponatremia |
| Study Type: | Observational |
| Study Design: | Observational Model: Cohort Time Perspective: Prospective |
| Official Title: | Institutional Registry of Hyponatremia |
Further study details as provided by Hospital Italiano de Buenos Aires:
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
| Sampling Method: | Non-Probability Sample |
Study Population
Adults with hyponatremia
Criteria
Inclusion Criteria:
- Over 17 years.
- At least a measure of central laboratory Na less than 130 mmol / l in patients without criteria for chronic hyponatremia or at least a measure of central laboratory Na greater than or equal to 150 mmol / l.
- First detection of sodium less than 130 mmol / l defined as exacerbation of chronic hyponatremia patients.
- Reepisodio defined as hyponatremia in patients who recovered the acute episode and again have a new episode of acute hyponatremia.
Exclusion Criteria:
- The refusal to register or to the informed consent process.
- Error in the measurement of sodium in the opinion of treating physician / recognized laboratory.
- Chronic renal patients on hemodialysis or peritoneal dialysis.
- Sodium determinations patients with cardiovascular surgery during cardiopulmonary bypass with intraoperative sodium determinations.
- Outpatients (excluding patients with PS on guard and spontaneous demand, see definitions).
- Patients treated (removal of blood and determination of serum sodium) in San Justo.
Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT01370473
Contacts
| Contact: Diego H Giunta, MD | 5411-9590200 ext 4419 | diego.giunta@hospitalitaliano.org.ar |
Locations
| Argentina | |
| HOspital Italiano de Buenos Aires | Recruiting |
| Gascon 450, Buenos Aires, Argentina | |
| Contact: Diego H Giunta, MD 541149590200 ext 4419 diego.giunta@hospitalitaliano.org.ar | |
Sponsors and Collaborators
Hospital Italiano de Buenos Aires
More Information
No publications provided
| Responsible Party: | Diego Giunta, Hospital Italiano de Buenos Aires |
| ClinicalTrials.gov Identifier: | NCT01370473 History of Changes |
| Other Study ID Numbers: | 1050 |
| Study First Received: | May 2, 2011 |
| Last Updated: | June 9, 2011 |
| Health Authority: | Argentine: AMNAT |
Keywords provided by Hospital Italiano de Buenos Aires:
|
Hyponatremia |
Additional relevant MeSH terms:
|
Hyponatremia Water-Electrolyte Imbalance Metabolic Diseases |
ClinicalTrials.gov processed this record on May 22, 2013